| Literature DB >> 24360960 |
Renate Fritzsche1, Daniela Karra2, Keiryn L Bennett3, Foong Yee Ang4, Jacki E Heraud-Farlow1, Marco Tolino1, Michael Doyle1, Karl E Bauer4, Sabine Thomas5, Melanie Planyavsky3, Eric Arn2, Anetta Bakosova1, Kerstin Jungwirth2, Alexandra Hörmann1, Zsofia Palfi1, Julia Sandholzer1, Martina Schwarz1, Paolo Macchi2, Jacques Colinge3, Giulio Superti-Furga3, Michael A Kiebler6.
Abstract
Transport of RNAs to dendrites occurs in neuronal RNA granules, which allows local synthesis of specific proteins at active synapses on demand, thereby contributing to learning and memory. To gain insight into the machinery controlling dendritic mRNA localization and translation, we established a stringent protocol to biochemically purify RNA granules from rat brain. Here, we identified a specific set of interactors for two RNA-binding proteins that are known components of neuronal RNA granules, Barentsz and Staufen2. First, neuronal RNA granules are much more heterogeneous than previously anticipated, sharing only a third of the identified proteins. Second, dendritically localized mRNAs, e.g., Arc and CaMKIIα, associate selectively with distinct RNA granules. Third, our work identifies a series of factors with known roles in RNA localization, translational control, and RNA quality control that are likely to keep localized transcripts in a translationally repressed state, often in distinct types of RNPs.Entities:
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Year: 2013 PMID: 24360960 DOI: 10.1016/j.celrep.2013.11.023
Source DB: PubMed Journal: Cell Rep Impact factor: 9.423